ClinicalTrials.Veeva

Menu

Swipe Out Stroke (SOS): Feasibility of Using a Consumer Based Electronic Application to Improve Compliance With Weight Loss in Obese Minority Stroke Patients

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Stroke

Treatments

Behavioral: Usual Care
Behavioral: Food Journal
Behavioral: Mobile Application

Study type

Interventional

Funder types

Other

Identifiers

NCT02531074
HSC-MS-13-0608

Details and patient eligibility

About

This pilot study evaluates the use of a mobile application to improve weight loss in obese stroke patients. The investigators hypothesize that acute stroke patients who use the mobile application are more likely to achieve a minimum 5% weight reduction during the critical six months post-stroke, yielding considerable improvement in stroke risk factors.

Enrollment

56 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Ischemic or hemorrhagic stroke.
  2. Age 18-85 years.
  3. African-American or Hispanic.
  4. Modified Rankin Scale (mRS) of 0-3.
  5. Body Mass Index greater than 30 kg/m2.
  6. Currently taking prescription medication for diabetes mellitus, hypertension or hyperlipidemia.
  7. Willing to follow a healthy eating pattern and NOT use weight loss medications for the duration of the study.
  8. Personal ownership or caregiver ownership of a personal computer, SmartPhone or other SmartDevice (iPhone or Android platform) with Internet access.
  9. If patient has alexia, agraphia, acalculia, dementia or blindness - caregiver must be willing to complete the intervention.

Exclusion criteria

  1. Pre-existing disability with mRS > 4.
  2. Contraindications to weight loss (planning to become pregnant, history of an eating disorder).
  3. Steroid use for suspected vasculitis.
  4. Current or recent (past 6 months) participation in a weight loss program or use of weight loss medication.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

56 participants in 2 patient groups

Mobile Application plus Usual Care
Experimental group
Treatment:
Behavioral: Mobile Application
Behavioral: Usual Care
Food Journal plus Usual Care
Active Comparator group
Treatment:
Behavioral: Usual Care
Behavioral: Food Journal

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems